Bayesian network modeling of patterns of antibiotic cross-resistance by bacterial sample source

por Cherny, Stacey S., Chowers, Michal, Obolski, Uri
Publicado 2023

Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset

por Gui, Hongsheng, Li, Miaoxin, Sham, Pak C, Cherny, Stacey S
Publicado 2011

Deciphering the Causal Relationships Between Low Back Pain Complications, Metabolic Factors, and Comorbidities

por Tarabeih, Nader, Kalinkovich, Alexander, Shalata, Adel, Cherny, Stacey S, Livshits, Gregory
Publicado 2022

A Knowledge-Based Weighting Framework to Boost the Power of Genome-Wide Association Studies

por Li, Miao-Xin, Sham, Pak C., Cherny, Stacey S., Song, You-Qiang
Publicado 2010

The analysis of causal relationships between blood lipid levels and BMD

por Cherny, Stacey S., Freidin, Maxim B., Williams, Frances M. K., Livshits, Gregory
Publicado 2019

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets

por Li, Miao-Xin, Yeung, Juilian M. Y., Cherny, Stacey S., Sham, Pak C.
Publicado 2011

Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

por Kasher, Melody, Williams, Frances M K, Freidin, Maxim B, Malkin, Ida, Cherny, Stacey S, Livshits, Gregory
Publicado 2022

Homozygosity Mapping on a Single Patient—Identification of Homozygous Regions of Recent Common Ancestry by Using Population Data

por Zhang, Lu, Yang, Wanling, Ying, Dingge, Cherny, Stacey S, Hildebrandt, Friedhelm, Sham, Pak Chung, Lau, Yu Lung
Publicado 2011

Utility of the trnH–psbA Intergenic Spacer Region and Its Combinations as Plant DNA Barcodes: A Meta-Analysis

por Pang, Xiaohui, Liu, Chang, Shi, Linchun, Liu, Rui, Liang, Dong, Li, Huan, Cherny, Stacey S., Chen, Shilin
Publicado 2012

Using Glycosylated Hemoglobin to Define the Metabolic Syndrome in United States Adults

por Ong, Kwok Leung, Tso, Annette W.K., Lam, Karen S.L., Cherny, Stacey S., Sham, Pak Chung, Cheung, Bernard M.Y.
Publicado 2010

Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank

por Cherny, Stacey S., Livshits, Gregory, Wells, Helena R. R., Freidin, Maxim B., Malkin, Ida, Dawson, Sally J., Williams, Frances M. K.
Publicado 2020

Cost effective assay choice for rare disease study designs

por Campbell, Desmond D, Porsch, Robert M, Cherny, Stacey S, Capra, Valeria, Merello, Elisa, De Marco, Patrizia, Sham, Pak C, Garcia-Barceló, Maria-Mercè
Publicado 2015

A Mendelian randomization study of testosterone and cognition in men

por Zhao, Jie V., Lam, Tai Hing, Jiang, Chaoqiang, Cherny, Stacey S., Liu, Bin, Cheng, Kar Keung, Zhang, Weisen, Leung, Gabriel M., Schooling, C Mary
Publicado 2016

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis

por Wong, John K.L., Gui, Hongsheng, Kwok, Maxwell, Ng, Ping Wing, Lui, Colin H.T., Baum, Larry, Sham, Pak Chung, Kwan, Patrick, Cherny, Stacey S.
Publicado 2018

Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis

por Cheng, Guo, Chung, Patrick Ho-Yu, Chan, Edwin Kin-Wai, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2017

Gene Network Analysis of Candidate Loci for Human Anorectal Malformations

por Wong, Emily H. M., Ng, Chun-Laam, Lui, Vincent Chi-Hang, So, Man-ting, Cherny, Stacey S., Sham, Pak-Chung, Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2013

Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia

por Cui, Long, Wong, Emily Hoi-Man, Cheng, Guo, Firmato de Almeida, Manoel, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2013

Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study

por Trotta, Antonella, Iyegbe, Conrad, Di Forti, Marta, Sham, Pak C., Campbell, Desmond D., Cherny, Stacey S., Mondelli, Valeria, Aitchison, Katherine J., Murray, Robin M., Vassos, Evangelos, Fisher, Helen L.
Publicado 2016

A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

por Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publicado 2012

Correction: A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

por Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publicado 2012